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Illumina Inc paired end dna library preparation
Paired End Dna Library Preparation, supplied by Illumina Inc, used in various techniques. Bioz Stars score: 92/100, based on 27 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/paired end dna library preparation/product/Illumina Inc
Average 92 stars, based on 27 article reviews
Price from $9.99 to $1999.99
paired end dna library preparation - by Bioz Stars, 2019-10
92/100 stars

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Related Articles

Hybridization:

Article Title: Unraveling the genetic cause of a consanguineous family with unilateral coloboma and retinoschisis: expanding the phenotypic variability of RAX mutations
Article Snippet: DNA fragments were captured by hybridization to the capture panel via using the Exome Enrichment V5 Kit (Agilent Technologies, USA) and, sequenced on Illumina HiSeq. .. Briefly, DNA was sheared and subjected to Illumina paired-end DNA library preparation and sequenced using an Illumina HiSeq.

RNA Extraction:

Article Title: Identification and developmental expression profiling of putative alkaloid biosynthetic genes in Corydalis yanhusuo bulbs
Article Snippet: Paragraph title: RNA extraction, Illumina cDNA library construction and sequencing ... In order to obtain the reference transcriptome data for C. yanhusuo , equal quantities of high-quality total RNA from the above three bulb stages were pooled for Illumina paired-end cDNA library preparation.

Selection:

Article Title: Sixteen diverse laboratory mouse reference genomes define strain specific haplotypes and novel functional loci
Article Snippet: Sheared DNA was subjected to Illumina paired-end DNA library preparation and PCR-amplified for six cycles. .. Illumina sequencing compatible Mate Pair libraries were created at 3 and 6 Kb according to the Sanger method .

Sample Prep:

Article Title: Sixteen diverse laboratory mouse reference genomes define strain specific haplotypes and novel functional loci
Article Snippet: Sheared DNA was subjected to Illumina paired-end DNA library preparation and PCR-amplified for six cycles. .. Illumina sequencing compatible Mate Pair libraries were created at 3 and 6 Kb according to the Sanger method .

Article Title: Unraveling the genetic cause of a consanguineous family with unilateral coloboma and retinoschisis: expanding the phenotypic variability of RAX mutations
Article Snippet: The genomic DNA was sheared into 100–300 base pairs and used to generate Illumina libraries in agreement with the manufacturer’s sample preparation protocol, including end-pair, adenylation, and adapter ligation. .. Briefly, DNA was sheared and subjected to Illumina paired-end DNA library preparation and sequenced using an Illumina HiSeq.

Magnetic Beads:

Article Title: Sixteen diverse laboratory mouse reference genomes define strain specific haplotypes and novel functional loci
Article Snippet: For the paired-end libraries, 1-3 μg DNA was sheared to 100 to 1,000 bp using a Covaris E210 or LE220 (Covaris, Woburn, MA, USA) and size selected (350 to 450 bp) using magnetic beads (Ampure XP; Beckman Coulter). .. Sheared DNA was subjected to Illumina paired-end DNA library preparation and PCR-amplified for six cycles.

Article Title: Sequencing and characterization of the FVB/NJ mouse genome
Article Snippet: DNA (1 to 3 μg) was sheared to 100 to 1,000 bp using a Covaris E210 or LE220 (Covaris, Woburn, MA, USA) and size selected (350 to 450 bp) using magnetic beads (Ampure XP; Beckman Coulter). .. Sheared DNA was subjected to Illumina paired-end DNA library preparation and PCR-amplified for six cycles.

Article Title: Identification and developmental expression profiling of putative alkaloid biosynthetic genes in Corydalis yanhusuo bulbs
Article Snippet: In order to obtain the reference transcriptome data for C. yanhusuo , equal quantities of high-quality total RNA from the above three bulb stages were pooled for Illumina paired-end cDNA library preparation. .. For digital expression profiling of genes during bulb development, separate RNA samples from all three stages were used for Illumina single-end cDNA library preparation.

Article Title: Synthetic viability genomic screening defines Sae2 function in DNA repair
Article Snippet: DNA (1–3 μg) was sheared to 100–1,000 bp by using a Covaris E210 or LE220 (Covaris, Woburn, MA, USA) and size-selected (350–450 bp) with magnetic beads (Ampure XP; Beckman Coulter). .. Sheared DNA was subjected to Illumina paired-end DNA library preparation and PCR-amplified for six cycles.

Isolation:

Article Title: Generation and Characterisation of a Pax8-CreERT2 Transgenic Line and a Slc22a6-CreERT2 Knock-In Line for Inducible and Specific Genetic Manipulation of Renal Tubular Epithelial Cells
Article Snippet: Images were captured using the SmartCapture software (Digital Scientific, UK) and metaphases were karyotyped using the SmartType Karyotyper software (Digital Scientific). .. Sheared genomic DNA isolated from the liver of a Pax8 -CreERT2 transgenic mouse (1 μg) was subjected to Illumina paired-end DNA library preparation and PCR-amplified for six cycles. .. Amplified libraries were sequenced using the HiSeq platform (Illumina) according to the manufacturer’s protocol.

Ligation:

Article Title: Unraveling the genetic cause of a consanguineous family with unilateral coloboma and retinoschisis: expanding the phenotypic variability of RAX mutations
Article Snippet: The genomic DNA was sheared into 100–300 base pairs and used to generate Illumina libraries in agreement with the manufacturer’s sample preparation protocol, including end-pair, adenylation, and adapter ligation. .. Briefly, DNA was sheared and subjected to Illumina paired-end DNA library preparation and sequenced using an Illumina HiSeq.

Article Title: Identification and developmental expression profiling of putative alkaloid biosynthetic genes in Corydalis yanhusuo bulbs
Article Snippet: In order to obtain the reference transcriptome data for C. yanhusuo , equal quantities of high-quality total RNA from the above three bulb stages were pooled for Illumina paired-end cDNA library preparation. .. Briefly, Illumina mRNA-seq library construction was as follows: mRNA was purified from 20 μg of DNaseI-treated total RNA with a RIN of ≥8 using oligo(dT) magnetic beads and then sheared into short fragments by heat treatment in fragmentation buffer.

Polymerase Chain Reaction:

Article Title: Sixteen diverse laboratory mouse reference genomes define strain specific haplotypes and novel functional loci
Article Snippet: For the paired-end libraries, 1-3 μg DNA was sheared to 100 to 1,000 bp using a Covaris E210 or LE220 (Covaris, Woburn, MA, USA) and size selected (350 to 450 bp) using magnetic beads (Ampure XP; Beckman Coulter). .. Sheared DNA was subjected to Illumina paired-end DNA library preparation and PCR-amplified for six cycles. .. Amplified libraries were sequenced using the Illumina HiSeq platform as paired-end 100 base reads according to the manufacturer's protocol.

Article Title: Sequencing and characterization of the FVB/NJ mouse genome
Article Snippet: DNA (1 to 3 μg) was sheared to 100 to 1,000 bp using a Covaris E210 or LE220 (Covaris, Woburn, MA, USA) and size selected (350 to 450 bp) using magnetic beads (Ampure XP; Beckman Coulter). .. Sheared DNA was subjected to Illumina paired-end DNA library preparation and PCR-amplified for six cycles. .. Amplified libraries were sequenced using the HiSeq platform (Illumina) as paired-end 100 base reads according to the manufacturer's protocol.

Article Title: Identification and developmental expression profiling of putative alkaloid biosynthetic genes in Corydalis yanhusuo bulbs
Article Snippet: In order to obtain the reference transcriptome data for C. yanhusuo , equal quantities of high-quality total RNA from the above three bulb stages were pooled for Illumina paired-end cDNA library preparation. .. In order to obtain the reference transcriptome data for C. yanhusuo , equal quantities of high-quality total RNA from the above three bulb stages were pooled for Illumina paired-end cDNA library preparation.

Article Title: Generation and Characterisation of a Pax8-CreERT2 Transgenic Line and a Slc22a6-CreERT2 Knock-In Line for Inducible and Specific Genetic Manipulation of Renal Tubular Epithelial Cells
Article Snippet: Images were captured using the SmartCapture software (Digital Scientific, UK) and metaphases were karyotyped using the SmartType Karyotyper software (Digital Scientific). .. Sheared genomic DNA isolated from the liver of a Pax8 -CreERT2 transgenic mouse (1 μg) was subjected to Illumina paired-end DNA library preparation and PCR-amplified for six cycles. .. Amplified libraries were sequenced using the HiSeq platform (Illumina) according to the manufacturer’s protocol.

Article Title: Synthetic viability genomic screening defines Sae2 function in DNA repair
Article Snippet: DNA (1–3 μg) was sheared to 100–1,000 bp by using a Covaris E210 or LE220 (Covaris, Woburn, MA, USA) and size-selected (350–450 bp) with magnetic beads (Ampure XP; Beckman Coulter). .. Sheared DNA was subjected to Illumina paired-end DNA library preparation and PCR-amplified for six cycles. .. Amplified libraries were sequenced with the HiSeq platform (Illumina) as paired-end 100 base reads according to the manufacturer's protocol.

Article Title: ISPD gene mutations are a common cause of congenital and limb-girdle muscular dystrophies
Article Snippet: Sheared DNA was subjected to Illumina paired-end DNA library preparation and enriched for target sequences (Agilent Technologies; Human All Exon 50 Mb-ELID S02972011) according to the manufacturer’s recommendations (Agilent Technologies; SureSelectXT Automated Target Enrichment for Illumina Paired-End Multiplexed Sequencing). .. Sheared DNA was subjected to Illumina paired-end DNA library preparation and enriched for target sequences (Agilent Technologies; Human All Exon 50 Mb-ELID S02972011) according to the manufacturer’s recommendations (Agilent Technologies; SureSelectXT Automated Target Enrichment for Illumina Paired-End Multiplexed Sequencing).

Generated:

Article Title: Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel
Article Snippet: Sheared DNA was size subjected to Illumina paired-end DNA library preparation. .. Following size selection (300–500 bp insert size), DNA libraries were sequenced using the Illumina HiSeq platform as paired-end 100 base reads according to manufacturer's protocol.

Article Title: Generation and Characterisation of a Pax8-CreERT2 Transgenic Line and a Slc22a6-CreERT2 Knock-In Line for Inducible and Specific Genetic Manipulation of Renal Tubular Epithelial Cells
Article Snippet: Sheared genomic DNA isolated from the liver of a Pax8 -CreERT2 transgenic mouse (1 μg) was subjected to Illumina paired-end DNA library preparation and PCR-amplified for six cycles. .. Amplified libraries were sequenced using the HiSeq platform (Illumina) according to the manufacturer’s protocol.

Mouse Assay:

Article Title: Sixteen diverse laboratory mouse reference genomes define strain specific haplotypes and novel functional loci
Article Snippet: All DNA was obtained from the Jackson Laboratories from female mice ( ). .. Sheared DNA was subjected to Illumina paired-end DNA library preparation and PCR-amplified for six cycles.

Produced:

Article Title: Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel
Article Snippet: Sheared DNA was size subjected to Illumina paired-end DNA library preparation. .. Data generated at the Sanger Institute and BGI were aligned to the human reference separately by the respective centres.

Sequencing:

Article Title: Sixteen diverse laboratory mouse reference genomes define strain specific haplotypes and novel functional loci
Article Snippet: Paragraph title: Sequencing ... Sheared DNA was subjected to Illumina paired-end DNA library preparation and PCR-amplified for six cycles.

Article Title: Whole exome sequencing identifies mTOR and KEAP1 as potential targets for radiosensitization of HNSCC cells refractory to EGFR and β1 integrin inhibition
Article Snippet: Paragraph title: Whole exome sequencing ... Sheared DNA was subjected to Illumina paired-end DNA library preparation.

Article Title: Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel
Article Snippet: Paragraph title: Sequence data production ... Sheared DNA was size subjected to Illumina paired-end DNA library preparation.

Article Title: Sequencing and characterization of the FVB/NJ mouse genome
Article Snippet: Sheared DNA was subjected to Illumina paired-end DNA library preparation and PCR-amplified for six cycles. .. Sheared DNA was subjected to Illumina paired-end DNA library preparation and PCR-amplified for six cycles.

Article Title: Independent impacts of aging on mitochondrial DNA quantity and quality in humans
Article Snippet: Whole genome sequencing and subsequent read mapping of the TwinsUK cohorts were accomplished by the UK10K project [ ]. .. Briefly, DNA (1–3 μg) extracted from PBMCs was sheared to 100–1000 bp, and sheared DNA was sent to Illumina paired-end DNA library preparation.

Article Title: Unraveling the genetic cause of a consanguineous family with unilateral coloboma and retinoschisis: expanding the phenotypic variability of RAX mutations
Article Snippet: Paragraph title: Whole exome sequencing and analyses ... Briefly, DNA was sheared and subjected to Illumina paired-end DNA library preparation and sequenced using an Illumina HiSeq.

Article Title: Collapsed methylation quantitative trait loci analysis for low frequency and rare variants
Article Snippet: Sequencing was performed at both the Wellcome Trust Sanger Institute (WTSI) and the Beijing Genomics Institute (BGI). .. Sheared DNA was size subjected to Illumina paired-end DNA library preparation.

Article Title: Identification and developmental expression profiling of putative alkaloid biosynthetic genes in Corydalis yanhusuo bulbs
Article Snippet: Paragraph title: RNA extraction, Illumina cDNA library construction and sequencing ... In order to obtain the reference transcriptome data for C. yanhusuo , equal quantities of high-quality total RNA from the above three bulb stages were pooled for Illumina paired-end cDNA library preparation.

Article Title: Generation and Characterisation of a Pax8-CreERT2 Transgenic Line and a Slc22a6-CreERT2 Knock-In Line for Inducible and Specific Genetic Manipulation of Renal Tubular Epithelial Cells
Article Snippet: Sheared genomic DNA isolated from the liver of a Pax8 -CreERT2 transgenic mouse (1 μg) was subjected to Illumina paired-end DNA library preparation and PCR-amplified for six cycles. .. Paired-end, 75 base reads were generated to an average of 3.5 fold coverage across the genome.

Article Title: Incorporating Non-Coding Annotations into Rare Variant Analysis
Article Snippet: Paragraph title: Sequencing Data ... Sheared DNA was size subjected to Illumina paired-end DNA library preparation.

Article Title: A Protein Domain and Family Based Approach to Rare Variant Association Analysis
Article Snippet: Paragraph title: Sequencing Data ... Sheared DNA was size subjected to Illumina paired-end DNA library preparation.

Article Title: A pathway-centric approach to rare variant association analysis
Article Snippet: Paragraph title: Sequencing data ... Sheared DNA was size subjected to Illumina paired-end DNA library preparation.

Article Title: Exome Sequencing and Genotyping Identify a Rare Variant in NLRP7 Gene Associated With Ulcerative Colitis
Article Snippet: Paragraph title: 2.2. Exome sequencing analysis ... A total of 3 µg of genomic DNA was sheared to a mean fragment size of 150 bp [Covaris], and the fragments used for Illumina paired-end DNA library preparation and enrichment for target sequences [SureSelect Human All Exon 50Mb kit, Agilent].

Article Title: Synthetic viability genomic screening defines Sae2 function in DNA repair
Article Snippet: Sheared DNA was subjected to Illumina paired-end DNA library preparation and PCR-amplified for six cycles. .. Sheared DNA was subjected to Illumina paired-end DNA library preparation and PCR-amplified for six cycles.

Article Title: ISPD gene mutations are a common cause of congenital and limb-girdle muscular dystrophies
Article Snippet: Genomic DNA (1–3 μg) was sheared to 100–400 bp using a Covaris E210 or LE220 ultarsonicator. .. Sheared DNA was subjected to Illumina paired-end DNA library preparation and enriched for target sequences (Agilent Technologies; Human All Exon 50 Mb-ELID S02972011) according to the manufacturer’s recommendations (Agilent Technologies; SureSelectXT Automated Target Enrichment for Illumina Paired-End Multiplexed Sequencing). .. Enriched libraries were sequenced using the HiSeq™ platform (IIIumina) as paired-end 75-bp reads according to the manufacturer’s protocol.

Article Title: NDUFA4 Mutations Underlie Dysfunction of a Cytochrome c Oxidase Subunit Linked to Human Neurological Disease
Article Snippet: DNA (1–3 μg) was sheared to 100–400 bp using a Covaris E210 or LE220 (Covaris). .. Sheared DNA was subjected to Illumina paired-end DNA library preparation and enriched for target sequences (Agilent Technologies; Human All Exon 50 Mb - ELID S02972011) according to manufacturer’s recommendations (Agilent; SureSelectXT Automated Target Enrichment for Illumina Paired-End Multiplexed Sequencing). .. Enriched libraries were sequenced using the HiSeq platform (Illumina) as paired-end 75 base reads according to manufacturer’s protocol.

Article Title: Migrating partial seizures of infancy: expansion of the electroclinical, radiological and pathological disease spectrum
Article Snippet: Paragraph title: Whole exome sequencing ... DNA was sheared to fragments of 100–400 bp for Illumina paired-end DNA library preparation, then enriched for target sequences according to the manufacturer’s recommendations.

Article Title: Combined exome and whole-genome sequencing identifies mutations in ARMC4 as a cause of primary ciliary dyskinesia with defects in the outer dynein arm
Article Snippet: In parallel, whole-genome sequencing (WGS) was performed as part of the UK10K project in the two unaffected, obligate carrier parents of a consanguineous Pakistani PCD family PCD-141 (individuals I:1 and I:2 figure 1A), since material from their affected offspring was not sufficient for exome sequencing. .. For WGS, approximately 3 µg of genomic DNA was sheared to 100–1000 bp (Covaris) and the sheared DNA subjected to Illumina Paired-end DNA library preparation.

Random Hexamer Labeling:

Article Title: Identification and developmental expression profiling of putative alkaloid biosynthetic genes in Corydalis yanhusuo bulbs
Article Snippet: In order to obtain the reference transcriptome data for C. yanhusuo , equal quantities of high-quality total RNA from the above three bulb stages were pooled for Illumina paired-end cDNA library preparation. .. Briefly, Illumina mRNA-seq library construction was as follows: mRNA was purified from 20 μg of DNaseI-treated total RNA with a RIN of ≥8 using oligo(dT) magnetic beads and then sheared into short fragments by heat treatment in fragmentation buffer.

Amplification:

Article Title: Unraveling the genetic cause of a consanguineous family with unilateral coloboma and retinoschisis: expanding the phenotypic variability of RAX mutations
Article Snippet: 2000 Analyzers for 90 cycles per read following purification and amplification. .. Briefly, DNA was sheared and subjected to Illumina paired-end DNA library preparation and sequenced using an Illumina HiSeq.

Article Title: Identification and developmental expression profiling of putative alkaloid biosynthetic genes in Corydalis yanhusuo bulbs
Article Snippet: In order to obtain the reference transcriptome data for C. yanhusuo , equal quantities of high-quality total RNA from the above three bulb stages were pooled for Illumina paired-end cDNA library preparation. .. Cleaved mRNA fragments were reverse transcribed into the first cDNA strands using random hexamer primers followed by the second-strand cDNA synthesis using DNA polymerase I and RNase H. The dscDNAs were purified using a QiaQuick PCR extraction kit (Qiagen), washed with the elution buffer and followed with end repair, Poly (A) tailing addition and sequencing adapter ligation.

cDNA Library Assay:

Article Title: Identification and developmental expression profiling of putative alkaloid biosynthetic genes in Corydalis yanhusuo bulbs
Article Snippet: Total RNA was extracted using TRIplant reagent (BioTeke, Beijing, China) following the manufacturer’s instructions, quantified spectrophotometrically at 260 nm and submitted to the Beijing Genomics Institute (BGI, Shenzhen, China) for Illumina mRNA library construction and HiSeq™ 2000 sequencing. .. In order to obtain the reference transcriptome data for C. yanhusuo , equal quantities of high-quality total RNA from the above three bulb stages were pooled for Illumina paired-end cDNA library preparation. .. For digital expression profiling of genes during bulb development, separate RNA samples from all three stages were used for Illumina single-end cDNA library preparation.

DNA Sequencing:

Article Title: Sequencing and characterization of the FVB/NJ mouse genome
Article Snippet: Paragraph title: DNA sequencing and read alignment ... Sheared DNA was subjected to Illumina paired-end DNA library preparation and PCR-amplified for six cycles.

Article Title: Generation and Characterisation of a Pax8-CreERT2 Transgenic Line and a Slc22a6-CreERT2 Knock-In Line for Inducible and Specific Genetic Manipulation of Renal Tubular Epithelial Cells
Article Snippet: Paragraph title: DNA sequencing ... Sheared genomic DNA isolated from the liver of a Pax8 -CreERT2 transgenic mouse (1 μg) was subjected to Illumina paired-end DNA library preparation and PCR-amplified for six cycles.

Article Title: Synthetic viability genomic screening defines Sae2 function in DNA repair
Article Snippet: Paragraph title: Whole-genome paired-end DNA sequencing and data analysis ... Sheared DNA was subjected to Illumina paired-end DNA library preparation and PCR-amplified for six cycles.

Modification:

Article Title: Generation and Characterisation of a Pax8-CreERT2 Transgenic Line and a Slc22a6-CreERT2 Knock-In Line for Inducible and Specific Genetic Manipulation of Renal Tubular Epithelial Cells
Article Snippet: Sheared genomic DNA isolated from the liver of a Pax8 -CreERT2 transgenic mouse (1 μg) was subjected to Illumina paired-end DNA library preparation and PCR-amplified for six cycles. .. Paired-end, 75 base reads were generated to an average of 3.5 fold coverage across the genome.

Transgenic Assay:

Article Title: Generation and Characterisation of a Pax8-CreERT2 Transgenic Line and a Slc22a6-CreERT2 Knock-In Line for Inducible and Specific Genetic Manipulation of Renal Tubular Epithelial Cells
Article Snippet: Images were captured using the SmartCapture software (Digital Scientific, UK) and metaphases were karyotyped using the SmartType Karyotyper software (Digital Scientific). .. Sheared genomic DNA isolated from the liver of a Pax8 -CreERT2 transgenic mouse (1 μg) was subjected to Illumina paired-end DNA library preparation and PCR-amplified for six cycles. .. Amplified libraries were sequenced using the HiSeq platform (Illumina) according to the manufacturer’s protocol.

Purification:

Article Title: Unraveling the genetic cause of a consanguineous family with unilateral coloboma and retinoschisis: expanding the phenotypic variability of RAX mutations
Article Snippet: 2000 Analyzers for 90 cycles per read following purification and amplification. .. Briefly, DNA was sheared and subjected to Illumina paired-end DNA library preparation and sequenced using an Illumina HiSeq.

Article Title: Identification and developmental expression profiling of putative alkaloid biosynthetic genes in Corydalis yanhusuo bulbs
Article Snippet: In order to obtain the reference transcriptome data for C. yanhusuo , equal quantities of high-quality total RNA from the above three bulb stages were pooled for Illumina paired-end cDNA library preparation. .. In order to obtain the reference transcriptome data for C. yanhusuo , equal quantities of high-quality total RNA from the above three bulb stages were pooled for Illumina paired-end cDNA library preparation.

Variant Assay:

Article Title: Collapsed methylation quantitative trait loci analysis for low frequency and rare variants
Article Snippet: Sheared DNA was size subjected to Illumina paired-end DNA library preparation. .. Sheared DNA was size subjected to Illumina paired-end DNA library preparation.

Article Title: Incorporating Non-Coding Annotations into Rare Variant Analysis
Article Snippet: Sheared DNA was size subjected to Illumina paired-end DNA library preparation. .. Sheared DNA was size subjected to Illumina paired-end DNA library preparation.

Article Title: A Protein Domain and Family Based Approach to Rare Variant Association Analysis
Article Snippet: Sheared DNA was size subjected to Illumina paired-end DNA library preparation. .. Sheared DNA was size subjected to Illumina paired-end DNA library preparation.

Article Title: A pathway-centric approach to rare variant association analysis
Article Snippet: Sheared DNA was size subjected to Illumina paired-end DNA library preparation. .. Sheared DNA was size subjected to Illumina paired-end DNA library preparation.

Software:

Article Title: Exome Sequencing and Genotyping Identify a Rare Variant in NLRP7 Gene Associated With Ulcerative Colitis
Article Snippet: A total of 3 µg of genomic DNA was sheared to a mean fragment size of 150 bp [Covaris], and the fragments used for Illumina paired-end DNA library preparation and enrichment for target sequences [SureSelect Human All Exon 50Mb kit, Agilent]. .. A total of 3 µg of genomic DNA was sheared to a mean fragment size of 150 bp [Covaris], and the fragments used for Illumina paired-end DNA library preparation and enrichment for target sequences [SureSelect Human All Exon 50Mb kit, Agilent].

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    Illumina Inc paired end dna library preparation
    Paired End Dna Library Preparation, supplied by Illumina Inc, used in various techniques. Bioz Stars score: 92/100, based on 27 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/paired end dna library preparation/product/Illumina Inc
    Average 92 stars, based on 27 article reviews
    Price from $9.99 to $1999.99
    paired end dna library preparation - by Bioz Stars, 2019-10
    92/100 stars
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